Scleroderma

Dr Andrew Dixon and A.Prof Frank Gaillard et al.

Scleroderma, also known as systemic sclerosis, is an autoimmune connective tissue disorder characterized by multisystem fibrosis and soft tissue calcification. As such, it affects many separate organ systems, which are discussed separately:

The remainder of this article is a general discussion of scleroderma.

Although presentation in childhood is indeed recognized 1, scleroderma is considered a disease of middle age (30-50 years of age) 3,4. There is a strong female predilection (F:M 3:1), even more pronounced during reproductive years (F:M 10:1) 2.

Clinical manifestation depends on which systems are predominantly involved. It should be noted that the majority of patients 70-97% develop an arthropathy that mostly affects the fingers, wrists, and ankles 3,5. Esophageal involvement is common, occurring in approximately 80% of patients 5. Although 90% of patients have pulmonary involvement histologically, only a minority are symptomatic 4,5.

The disease is characterized by widespread deposition of collagen and other extracellular matrix proteins. This is believed to occur as a result of an abnormal immune response. Small vessels are involved early in the disease, accounting for the involvement of organs with a dense capillary network. This results in perivascular fibrosis and gradual luminal stenosis 5.

Serological markers include 3:

  • elevated erythrocyte sedimentation rate (ESR)
  • rheumatoid factor (RF): positive in 30-40%
  • antinuclear antibodies (ANA): 35-96%
  • anti SCL-70: 30-70% (particularly in diffuse disease)
  • anti-centromere antibodies: 20-40% (particularly in limited disease)
  • antitopoisomerase I

These are best discussed under manifestations of individual systems. Please refer to respective subsections.

No cure for scleroderma exists. Treatment aims to reduce systemic involvement and target particular symptomatic organ systems. For targeted therapy, please refer to the articles that pertain to scleroderma and the particular body system.

Systemic medication aimed at reducing the deposition of fibrous tissue and at reducing inflammation has been tried with limited success 5.

Overall prognosis is variable, depending on the organ(s) involved and the severity. For patients with limited cutaneous involvement, the 10-year survival is approximately 75%. However, patients with diffuse involvement have a 10-year survival closer to 55% 5.

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Article information

rID: 2028
Synonyms or Alternate Spellings:
  • Progressive systemic sclerosis (PSS)
  • Systemic sclerosis
  • Progressive systemic sclerosis

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Cases and figures

  • Case 1
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  • Case 2
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  • Csse 3: with small bowel involvement
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  • Scleroderma
    Case 4
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  • Case 5
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  • Case 6
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  •  Case 7
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  • Case 8
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  • Case 9
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